Pickleball for Parkinson's of Connecticut is a 501(c)(3) (*** Application Pending) nonprofit using the joy of pickleball to help people living with Parkinson's move better, feel stronger, and stay connected — while raising funds for research toward a cure.
Parkinson's disease (PD) is a progressive neurological disorder that primarily affects movement, though it can also impact mental health, sleep, and cognitive function. It occurs when nerve cells in a specific part of the brain — the substantia nigra — become impaired or die.
These cells normally produce dopamine, the chemical messenger that allows the brain to coordinate smooth, controlled muscle movements. When dopamine levels drop significantly, physical symptoms begin to appear. Symptoms usually start gradually and worsen over time.
The exact cause is still unknown, but experts believe it is a combination of:
There is currently no cure for Parkinson's, but treatment can significantly improve quality of life. The standard toolkit includes medication (typically Levodopa with Carbidopa), Deep Brain Stimulation surgery in some cases, and physical, occupational, and speech therapy.
Increasingly, exercise is viewed not just as a supplement to PD treatment, but as a form of "medicine" that can directly influence brain health and the disease's progression. Studies show regular, targeted physical activity helps in three distinct ways:
Exercise helps the brain "rewire" itself.
Targeted activity addresses the physical challenges of PD.
Exercise reaches symptoms that aren't movement-related.
Pickleball checks every box the research points to: it's aerobic, it requires fast reaction time and coordination, it involves multi-directional movement, and it's intensely social. The court is small, the rules are simple, and the learning curve is forgiving — so people newly diagnosed and people years in can play side by side.
Just as importantly, pickleball is fun. The single best predictor of whether someone will keep exercising is whether they enjoy it. Our weekly play group is built around that fact.
My Parkinson's story started on a bright sunny day in 2014. I had just started on a walk with my wife with the sun at my back. While looking at my shadow in front of me, I noticed that my left arm was not swinging in stride normally. I pointed this out to my wife, and she recommended that I see a doctor to assess the lack of arm swing.
After many tests and neurology exams, it was determined that I had Parkinson's disease. On August 1, 2015 I officially started taking my dopamine medications.
P4PCT exists to share that experience with others living with Parkinson's in our community — and to channel the energy of the game into research that helps everyone affected by the disease.